A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551878



Internal ID325298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52839197..52839197hg38UCSC Ensembl
chr4:53705364..53705364hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551878
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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